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| Product NDC Code | 76176-118 | ||||
|---|---|---|---|---|---|
| Drug Name | Sanitaxe antibacterial amber hand |
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| Type | Brand | ||||
| Active Ingredients |
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| Route | TOPICAL | ||||
| Dosage Form | LIQUID | ||||
| RxCUI drug identifier | 1941461 | ||||
| Application Number | part333A | ||||
| Labeler Name | NINGBO LIYUAN DAILY CHEMICAL PRODUCTS CO., LTD. | ||||
| Packages |
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Active ingredient
A list of the active, medicinal ingredients in the drug product.Drug Facts Active ingredients Chloroxylenol 0.1 percent
Dosage and administration
Information about the drug product’s dosage and administration recommendations, including starting dose, dose range, titration regimens, and any other clinically sigificant information that affects dosing recommendations.Directions wet hands. Apply palmful to hands. Scrub thoroughly. Rinse.
Inactive ingredient
A list of inactive, non-medicinal ingredients in a drug product.Inactive ingredients Water (Aqua), Sodium Laureth Sulfate, Cocamidopropyl Betaine, Sodium Lauryl Sulfate, Glycerin, Sodium Chloride, Fragrance, Citric Acid, PEG-150 Distearate, Methylchloroisothiazolinone, Methylisothiazolinone, FD&C Yellow No.5.
Indications and usage
A statement of each of the drug products indications for use, such as for the treatment, prevention, mitigation, cure, or diagnosis of a disease or condition, or of a manifestation of a recognized disease or condition, or for the relief of symptoms associated with a recognized disease or condition. This field may also describe any relevant limitations of use.Uses for handwashing to eliminate bacterial and germs on the skin.
Purpose
Information about the drug product’s indications for use.Purpose Antibacterial
Spl product data elements
Usually a list of ingredients in a drug product.SANITAXE ANTIBACTERIAL AMBER HAND Chloroxylenol WATER FD&C YELLOW NO. 5 SODIUM LAURETH SULFATE SODIUM CHLORIDE COCAMIDOPROPYL BETAINE SODIUM LAURYL SULFATE GLYCERIN CHLOROXYLENOL CHLOROXYLENOL CITRIC ACID ACETATE PEG-150 DISTEARATE METHYLCHLOROISOTHIAZOLINONE
Package label principal display panel
The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.label
Keep out of reach of children
Information pertaining to whether the product should be kept out of the reach of children, and instructions about what to do in the case of accidental contact or ingestion, if appropriate.Keep out of reach of children. Children must be supervised in use of this product.
Other safety information
Information about safe use and handling of the product that may not have been specified in another field.Other information store at 20 Degree Celsius (68 to 77 Fahrenheit). May discolor fabrics.
Stop use
Information about when use of the drug product should be discontinued immediately and a doctor consulted. Includes information about any signs of toxicity or other reactions that would necessitate immediately discontinuing use of the product.Stop use and ask a doctor if redness or irritation develops and persists for more than 72 hours.
Warnings
Information about serious adverse reactions and potential safety hazards, including limitations in use imposed by those hazards and steps that should be taken if they occur.Warnings For external use only. Do not apply around eyes. Do not use in ears and mouth. When using this product, avoid contact with eyes. In case of contact flush eyes with water.
Disclaimer: Do not rely on openFDA or Phanrmacy Near Me to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API